I am posting this article because last week a reader made his or her way to my Google blog by asking, "How can I recover from derealization?" By typing "derealization" into a search engine, you can find many good professionally-written articles discussing this symptom, and this clinical information can help you understand the phenomenon. However, my purpose in writing the following article is to help you see the symptom through my eyes, the eyes of a person recovering from C-PTSD. In addition to giving you a description of the phenomenon through the eyes of a client rather than a practitioner, I may be able to help you allay some fears you may have regarding derealization. At the end of this post you will find a link to a previous article I wrote on this topic. Embedded in the article is a link to a clear explanation of derealization. I believe that as you work to recover and heal your C-PTSD, you may find that incidences of derealization will become less frequent as your other symptoms fade–I say this based solely on my own experience. None of the clinical articles I have read has speculated on a connection between reduction of general PTSD symptoms and reduction in frequency of derealization incidents.
`Curiouser and curiouser!' cried Alice (she was so much surprised, that for the moment she quite forgot how to speak good English); `now I'm opening out like the largest telescope that ever was! Good-bye, feet!' (for when she looked down at her feet, they seemed to be almost out of sight, they were getting so far off). `Oh, my poor little feet, I wonder who will put on your shoes and stockings for you now, dears? I'm sure I shan't be able! I shall be a great deal too far off to trouble myself about you: you must manage the best way you can; --but I must be kind to them,' thought Alice, `or perhaps they won't walk the way I want to go! Let me see: I'll give them a new pair of boots every Christmas.' (From Alice's Adventures in Wonderland by Lewis Carroll, Project Gutenberg.)
The episodes came and went, and I said nothing to anyone about them. As time passed, they were simply part of my life--like eating, brushing my teeth, and doing schoolwork. By the time I was in high school, though, I seldom experienced the problem, and the derealization episodes faded into the past. When I entered college as an undergraduate, however, I was once again plagued by the symptoms, but as before, my fear rendered me unable to reach out for help. I thought, in fact, that there was no help for my condition, and I did not want to risk being labeled as "crazy" and locked away in an institution. Again, I felt there was nothing I could do but endure the symptoms and try to forget them.
After I graduated from college, I found a job, married, and had a baby. The symptoms did not return until late in my marriage, near the time in 1981 when I caught my husband abusing our daughter and reported him to the police. After that, I had episodes of derealization from time to time, but because they did not occur frequently, I simply got through them and tried not to think about them. As I look back, a pattern emerges: My episodes of derealization have occurred most frequently at periods in my life when my anxiety and stress have been most intense and when I have felt physically or emotionally threatened. This insight is supported by the information in the professionally-written articles I have read, such as this one-- http://www.ptsd.va.gov/professional/pages/Dissociative_Subtype_of_PTSD.asp
“If you hear a voice within you say “you cannot paint,” then by all means paint, and that voice will be silenced.” ~ Vincent Van Gogh, Dutch Painter
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